--- title: "Orthoscan, Inc. Recalls: Agency-Reported Status and History (Oct 1, 2026) | Is It on Recall" description: "Search Orthoscan, Inc. recall records, lots, firms and dates. Reported status can be incomplete; use the linked agency notice for current instructions." url: https://isitonrecall.com/brand/orthoscan-inc/ updated: 2026-10-01 site: "Is It on Recall" language: en --- [Home](https://isitonrecall.com/) / Brand archive # Orthoscan, Inc. recall records **7** reported ongoing 7 records in this archive. Latest source date Aug 8, 2024. FDA enforcement status can lag behind the recall lifecycle. An empty search or a reported termination is not a personal product-safety determination. Archive changed Oct 1, 2026. USDA FSIS records are unavailable; [check FSIS directly](https://www.fsis.usda.gov/recalls). [Source coverage and dates](https://isitonrecall.com/sources/). ## Records and reported status Aug 8, 2024 FDA device enforcement ### [Ziehm Solo. Digital Mobile C-arm](https://isitonrecall.com/recall/fda-device-z-0573-2025-ziehm-solo-digital-mobile-c-arm/) Ziehm Imaging, Inc., distributor, have been informed by manufacturer, Ziehm Imaging GmbH that installed devices may not fully meet the requirements of IEC 60601-2-54 and or 21 CFR 1020.32(c) with respect to wired hand switch may fail when being exposed to m... Class II Reported ongoing Distribution: U.S. (including Puerto Rico). [Official source for Ziehm Solo. Digital Mobile C-arm](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-0573-2025%22) Aug 8, 2024 FDA device enforcement ### [Ziehm Solo FD. Interventional fluoroscopic x-ray system](https://isitonrecall.com/recall/fda-device-z-0574-2025-ziehm-solo-fd-interventional-fluoroscopic-x-ray-system/) Ziehm Imaging, Inc., distributor, have been informed by manufacturer, Ziehm Imaging GmbH that installed devices may not fully meet the requirements of IEC 60601-2-54 and or 21 CFR 1020.32(c) with respect to wired hand switch may fail when being exposed to m... Class II Reported ongoing Distribution: U.S. (including Puerto Rico). [Official source for Ziehm Solo FD. Interventional fluoroscopic x-ray system](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-0574-2025%22) Aug 8, 2024 FDA device enforcement ### [Ziehm Vision system, x-ray, tomography, computed.](https://isitonrecall.com/recall/fda-device-z-0575-2025-ziehm-vision-system-x-ray-tomography-computed/) Ziehm Imaging, Inc., distributor, have been informed by manufacturer, Ziehm Imaging GmbH that installed devices may not fully meet the requirements of IEC 60601-2-54 and or 21 CFR 1020.32(c) with respect to wired hand switch may fail when being exposed to m... Class II Reported ongoing Distribution: U.S. (including Puerto Rico). [Official source for Ziehm Vision system, x-ray, tomography, computed.](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-0575-2025%22) Aug 8, 2024 FDA device enforcement ### [Ziehm Vision FD. Interventional fluoroscopic x-ray system](https://isitonrecall.com/recall/fda-device-z-0576-2025-ziehm-vision-fd-interventional-fluoroscopic-x-ray-system/) Ziehm Imaging, Inc., distributor, have been informed by manufacturer, Ziehm Imaging GmbH that installed devices may not fully meet the requirements of IEC 60601-2-54 and or 21 CFR 1020.32(c) with respect to wired hand switch may fail when being exposed to m... Class II Reported ongoing Distribution: U.S. (including Puerto Rico). [Official source for Ziehm Vision FD. Interventional fluoroscopic x-ray system](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-0576-2025%22) Aug 8, 2024 FDA device enforcement ### [Ziehm Vision R. Iterventional fluoroscopic x-ray system](https://isitonrecall.com/recall/fda-device-z-0577-2025-ziehm-vision-r-iterventional-fluoroscopic-x-ray-system/) Ziehm Imaging, Inc., distributor, have been informed by manufacturer, Ziehm Imaging GmbH that installed devices may not fully meet the requirements of IEC 60601-2-54 and or 21 CFR 1020.32(c) with respect to wired hand switch may fail when being exposed to m... Class II Reported ongoing Distribution: U.S. (including Puerto Rico). [Official source for Ziehm Vision R. Iterventional fluoroscopic x-ray system](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-0577-2025%22) Aug 8, 2024 FDA device enforcement ### [Ziehm Vision RFD. Interventional fluoroscopic x-ray system](https://isitonrecall.com/recall/fda-device-z-0578-2025-ziehm-vision-rfd-interventional-fluoroscopic-x-ray-system/) Ziehm Imaging, Inc., distributor, have been informed by manufacturer, Ziehm Imaging GmbH that installed devices may not fully meet the requirements of IEC 60601-2-54 and or 21 CFR 1020.32(c) with respect to wired hand switch may fail when being exposed to m... Class II Reported ongoing Distribution: U.S. (including Puerto Rico). [Official source for Ziehm Vision RFD. Interventional fluoroscopic x-ray system](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-0578-2025%22) Aug 8, 2024 FDA device enforcement ### [Ziehm Vision RFD 3D. Interventinoal fluoroscopic x-ray system](https://isitonrecall.com/recall/fda-device-z-0579-2025-ziehm-vision-rfd-3d-interventinoal-fluoroscopic-x-ray-system/) Ziehm Imaging, Inc., distributor, have been informed by manufacturer, Ziehm Imaging GmbH that installed devices may not fully meet the requirements of IEC 60601-2-54 and or 21 CFR 1020.32(c) with respect to wired hand switch may fail when being exposed to m... Class II Reported ongoing Distribution: U.S. (including Puerto Rico). [Official source for Ziehm Vision RFD 3D. Interventinoal fluoroscopic x-ray system](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-0579-2025%22) ## Reasons in these listed records - Ziehm Imaging, Inc., distributor, have been informed by manufacturer, Ziehm Imaging GmbH that installed devices may not fully meet the requirements of IEC 60601-2-54 and or 21 CFR 1020.32(c) with respect to wired hand switch may fail when being exposed to mechanical stress suc... These examples come from this result page and are not a ranking of every recall reason. ## Checking Orthoscan, Inc. ### Is there a recall on orthoscan, inc. right now? This archive contains 7 records, including 7 with agency-reported ongoing status. The status field can be incomplete or stale. Open the current official notice and match your exact product. ### How do I check my package or product? Compare the product, firm and lot, date, model or serial identifiers with the notice. [Use the label-check guide](https://isitonrecall.com/guides/read-lot-codes/) if you need help locating an identifier. ### Does a matching name mean every item is included? A name is a search match. The agency notice sets the affected products and identifiers. Do not assume that every item with the same name or brand belongs to the recall. ### What if the search finds no matching record? This search has source and keyword limits. Missing records or a missing lot code do not establish that a product is unaffected. [Check source coverage](https://isitonrecall.com/sources/) and the agency's current notices. ### Where can I find older records? Use [monthly archives](https://isitonrecall.com/archives/) or the local search. The initial import covers records dated from October 2021 where available; each source's actual first and latest dates appear on the coverage page. ## Keep checking [Search Orthoscan, Inc.](https://isitonrecall.com/check/?q=Orthoscan%2C%20Inc.) [Browse related products](https://isitonrecall.com/products/) [Review source dates](https://isitonrecall.com/sources/)